How Much Does a District Manager Medical Device make?
District Manager Medical Device made a median salary around $101,592 in December, 2024.
The best-paid 25 percent made $120,359 probably that year, while the lowest-paid 25 percent made around $83,751.
Salary ranges can vary widely depending on many important factors, including education, certifications, additional skills, the number of years you have spent in your profession.
With more online, real-time compensation data than any other website, Salary.com helps you determine your exact pay target.
Best-Paying Cities for District Manager Medical Device
The metropolitan areas that pay the highest salary in the District Manager Medical Device profession are Kansas City
, Riverside
, Saint Louis
, Independence
, Saint Ann
.
Kansas City, MO
|
$101,592
|
Riverside, MO
|
$101,592
|
Saint Louis, MO
|
$101,592
|
Independence, MO
|
$101,488
|
Saint Ann, MO
|
$101,488
|
Best-Paying States for District Manager Medical Device
The states and districts that pay District Manager Medical Device the highest salary are District of Columbia (around $115,497)
, California (around $114,460)
, New Jersey (around $113,733)
, Alaska (around $113,007)
, and Massachusetts (around $112,903)
.
Frequently Asked Questions for District Manager Medical Device
Q:
What is the salary range of District Manager Medical Device in Saint Louis, MO?
A:
In 2024
, the lowest-paid District Manager Medical Device in Saint Louis, MO earned an average annual salary of $83,751
, while the highest-paid made $120,359.
Q:
What is the salary for a District Manager Medical Device in California?
A:
District Manager Medical Device employed in California earned an average salary of $114,460 in 2024.
Relevant Jobs of District Manager Medical Device
Medical Device Engineering Manager manages the analysis and development of medical devices, equipment, or components to meet technical and functional specifications and standards. Provides technical direction to team members in designing, developing, and testing medical devices or components. Being a Medical Device Engineering Manager utilizes CAD software and other design and modeling tools to plan, develop, and improve medical devices or components. Oversees prototype testing to evaluate medical device performance, reliability, and safety and reviews data and analysis to develop improvements. Additionally, Medical Device Engineering Manager manages engineering projects through their entire lifecycle, including cost and requirement analysis, scheduling, and production. Establishes operational policies and guidelines to ensure products meet regulatory, safety, and quality requirements and standards. Stays abreast of new technologies and processes and implements changes to improve the organization's engineering capabilities. May require a master's degree. Typically reports to a director. The Medical Device Engineering Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. To be a Medical Device Engineering Manager typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes.
Medical Device Engineering Supervisor designs, develops, and enhances medical devices, equipment, or components to meet technical and functional specifications and standards. Utilizes CAD software and other design and modeling tools to evaluate design feasibility and communicate conceptual designs and specifications to stakeholders. Being a Medical Device Engineering Supervisor oversees prototype testing to evaluate medical device performance, reliability, and safety and collects and analyzes data for improvements. Implements mechanical and electrical engineering principles to analyze and troubleshoot malfunctions, identify root causes, and develop solutions. Additionally, Medical Device Engineering Supervisor researches and selects appropriate materials and processes to ensure product quality, performance, and manufacturability. Implements operational policies and guidelines to ensure products meet regulatory, safety, and quality requirements and standards. Develops modifications or fabrications to resolve production or assembly issues. Requires a bachelor's degree. Typically reports to a manager. The Medical Device Engineering Supervisor supervises a group of primarily para-professional level staffs. May also be a level above a supervisor within high volume administrative/production environments. Makes day-to-day decisions within or for a group/small department. Has some authority for personnel actions. To be a Medical Device Engineering Supervisor typically requires 3-5 years experience in the related area as an individual contributor. Thorough knowledge of functional area and department processes.
Medical Device Engineer III designs, develops, and enhances medical devices, equipment, or components to meet technical and functional specifications and standards. Utilizes CAD software and other design and modeling tools to evaluate design feasibility and communicate conceptual designs and specifications to stakeholders. Being a Medical Device Engineer III conducts prototype testing to evaluate medical device performance, reliability, and safety and collects and analyzes data for improvements. Utilizes mechanical and electrical engineering principles to analyze and troubleshoot malfunctions, identify root causes, and develop solutions. Additionally, Medical Device Engineer III identifies appropriate materials and processes to ensure product quality, performance, and manufacturability. Follows operational policies and guidelines to ensure products meet regulatory, safety, and quality requirements and standards. Develops modifications or fabrications to resolve production or assembly issues. Requires a bachelor's degree. Typically reports to a manager. The Medical Device Engineer III work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. To be a Medical Device Engineer III typically requires 4-7 years of related experience.
Medical Device Engineer VI designs, develops, and enhances medical devices, equipment, or components to meet technical and functional specifications and standards. Utilizes CAD software and other design and modeling tools to evaluate design feasibility and communicate conceptual designs and specifications to stakeholders. Being a Medical Device Engineer VI conducts prototype testing to evaluate medical device performance, reliability, and safety and collects and analyzes data for improvements. Utilizes mechanical and electrical engineering principles to analyze and troubleshoot malfunctions, identify root causes, and develop solutions. Additionally, Medical Device Engineer VI identifies appropriate materials and processes to ensure product quality, performance, and manufacturability. Follows operational policies and guidelines to ensure products meet regulatory, safety, and quality requirements and standards. Develops modifications or fabrications to resolve production or assembly issues. Requires a bachelor's degree. Typically reports to a manager. To be a Medical Device Engineer VI typically requires 12+ years of related experience. Achievement and depth of knowledge of specialization or field is the main differentiator. Advisory role on complex and challenging projects and initiatives. Recognized for deep technical and industry knowledge and innovative thinking. Provides thought leadership and guidance to a functional area and the organization.
Medical Device Engineer I designs, develops, and enhances medical devices, equipment, or components to meet technical and functional specifications and standards. Utilizes CAD software and other design and modeling tools to evaluate design feasibility and communicate conceptual designs and specifications to stakeholders. Being a Medical Device Engineer I conducts prototype testing to evaluate medical device performance, reliability, and safety and collects and analyzes data for improvements. Utilizes mechanical and electrical engineering principles to analyze and troubleshoot malfunctions, identify root causes, and develop solutions. Additionally, Medical Device Engineer I identifies appropriate materials and processes to ensure product quality, performance, and manufacturability. Follows operational policies and guidelines to ensure products meet regulatory, safety, and quality requirements and standards. Develops modifications or fabrications to resolve production or assembly issues. Requires a bachelor's degree. Typically reports to a manager. The Medical Device Engineer I work is closely managed. Works on projects/matters of limited complexity in a support role. To be a Medical Device Engineer I typically requires 0-2 years of related experience.